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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925572Generated: October 26, 2026

9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid (4-aminopyridin-3-yl)amide → HCID 67072884, compound

https://huagongshe.com/reaction/1925572

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid (4-aminopyridin-3-yl)amideHCID 67299358—
SolventAcetic AcidHCID 176—
ProductHCID 67072884HCID 6707288446.1%

Reaction Conditions

Temperature200 °C

Reaction Steps

In a 20 ml microwave reactor, a mixture of 256 mg of 9-oxo-9H-pyrrolo[1,2-a]indole-5-carboxylic acid (4-aminopyridin-3-yl)amide obtained according to the preceding stage, in 20 ml of glacial acetic acid, is heated at 200° C. for 30 minutes. The reaction medium is filtered through clarcel, washing being carried out with glacial acetic acid. The filtrate is evaporated to dryness under vacuum and the residue is taken up twice with toluene and each time re-evaporated to dryness under vacuum. The solid is triturated from isopropyl ether, filtered, and dried under vacuum at 40° C. overnight. 111 mg of 5-(3H-imidazo[4,5-c]pyridin-2-yl)pyrrolo[1,2-a]indol-9-one are obtained in the form of a solid, the characteristics of which are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178687B2
Source datasetuspto-grants-2012_05
ORD IDord-cd8eeddff9144481bd321ffc907f4d29
Source noteuspto-grants-2012_05